Homo sapiens (human): 1317
Help
Entry
1317 CDS
T01001
Symbol
SLC31A1, COPT1, CTR1, NSCT
Name
(RefSeq) solute carrier family 31 member 1
KO
K14686
solute carrier family 31 (copper transporter), member 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa01524
Platinum drug resistance
hsa04978
Mineral absorption
Disease
H02736
Neurodegeneration and seizures due to copper transport defect
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09154 Digestive system
04978 Mineral absorption
1317 (SLC31A1)
09160 Human Diseases
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
1317 (SLC31A1)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
1317 (SLC31A1)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC31: Copper transporter
1317 (SLC31A1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ctr
Motif
Other DBs
NCBI-GeneID:
1317
NCBI-ProteinID:
NP_001850
OMIM:
603085
HGNC:
11016
Ensembl:
ENSG00000136868
UniProt:
O15431
Structure
PDB
PDBj
LinkDB
All DBs
Position
9:113221544..113264492
Genome browser
AA seq
190 aa
AA seq
DB search
MDHSHHMGMSYMDSNSTMQPSHHHPTTSASHSHGGGDSSMMMMPMTFYFGFKNVELLFSG
LVINTAGEMAGAFVAVFLLAMFYEGLKIARESLLRKSQVSIRYNSMPVPGPNGTILMETH
KTVGQQMLSFPHLLQTVLHIIQVVISYFLMLIFMTYNGYLCIAVAAGAGTGYFLFSWKKA
VVVDITEHCH
NT seq
573 nt
NT seq
+upstream
nt +downstream
nt
atggatcattcccaccatatggggatgagctatatggactccaacagtaccatgcaacct
tctcaccatcacccaaccacttcagcctcacactcccatggtggaggagacagcagcatg
atgatgatgcctatgaccttctactttggctttaagaatgtggaactactgttttccggt
ttggtgatcaatacagctggagaaatggctggagcttttgtggcagtgtttttactagca
atgttctatgaaggactcaagatagcccgagagagcctgctgcgtaagtcacaagtcagc
attcgctacaattccatgcctgtcccaggaccaaatggaaccatccttatggagacacac
aaaactgttgggcaacagatgctgagctttcctcacctcctgcaaacagtgctgcacatc
atccaggtggtcataagctacttcctcatgctcatcttcatgacctacaacgggtacctc
tgcattgcagtagcagcaggggccggtacaggatacttcctcttcagctggaagaaggca
gtggtagtggatatcacagagcattgccattga
DBGET
integrated database retrieval system
